Leung A K L, Sharp P A
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Cold Spring Harb Symp Quant Biol. 2006;71:29-38. doi: 10.1101/sqb.2006.71.049.
microRNAs (miRNAs) represent a large set of master regulators of gene expression. They constitute 1-4% of human genes and probably regulate 30% of protein-encoding genes. These small regulatory RNAs act at a posttranscriptional level-mediating translational repression and/or mRNA degradation-through their association with Argonaute protein and target mRNAs. In this paper, we discuss various mechanisms by which miRNAs regulate posttranscriptionally, including their subcellular localization. Recent results indicate that the majority of miRNA-targeted and thus translationally repressed mRNA is probably distributed in the diffuse cytoplasm, even though a small fraction is concentrated in subcellular compartments, such as processing bodies or stress granules; notably, the stress granule localization of Argonaute depends on the presence of miRNAs. Here we discuss the structural requirement of these subcellular compartments in light of their potential miRNA functions.
微小RNA(miRNA)是基因表达的一大类主要调节因子。它们占人类基因的1 - 4%,可能调控30%的蛋白质编码基因。这些小的调节性RNA在转录后水平发挥作用,通过与AGO蛋白和靶mRNA结合来介导翻译抑制和/或mRNA降解。在本文中,我们讨论了miRNA在转录后水平进行调控的各种机制,包括它们的亚细胞定位。最近的研究结果表明,尽管一小部分miRNA靶向并因此被翻译抑制的mRNA集中在亚细胞区室,如加工小体或应激颗粒中,但大多数此类mRNA可能分布在弥漫性细胞质中;值得注意的是,AGO蛋白在应激颗粒中的定位取决于miRNA的存在。在此,我们根据这些亚细胞区室潜在的miRNA功能来讨论其结构要求。